Canonical Allele Identifier: CA3714906
Gene: PRRC2A HGNC NCBI

Linked Data

dbSNP Id: rs774689648
gnomAD v2: 6-31590643-A-T
gnomAD v4: 6-31622866-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622866A>T , CM000668.2:g.31622866A>T GRCh38
NC_000006.11:g.31590643A>T , CM000668.1:g.31590643A>T GRCh37
NC_000006.10:g.31698622A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.77A>T MANE Select ENSP00000365201.2:p.Tyr26Phe
ENST00000376007.8:c.77A>T ENSP00000365175.4:p.Tyr26Phe
ENST00000376033.2:c.77A>T ENSP00000365201.2:p.Tyr26Phe
ENST00000469577.5:n.136-1395A>T
NM_004638.3:c.77A>T NP_004629.3:p.Tyr26Phe
NM_080686.2:c.77A>T NP_542417.2:p.Tyr26Phe
XM_011514890.1:c.77A>T XP_011513192.1:p.Tyr26Phe
XM_017011274.1:c.77A>T XP_016866763.1:p.Tyr26Phe
NM_004638.4:c.77A>T MANE Select NP_004629.3:p.Tyr26Phe
NM_080686.3:c.77A>T NP_542417.2:p.Tyr26Phe